Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2251214
SYT1
0.827 0.040 12 79430071 intron variant A/G;T snv 7
rs1018381
DTNBP1
0.882 0.040 6 15656839 intron variant G/A snv 0.16 6
rs7157599
DEGS2
0.925 0.040 14 100159565 missense variant C/T snv 0.73 0.76 6
rs750331613
GRID2
0.882 0.040 4 93515346 missense variant C/T snv 4.8E-05 2.1E-05 5
rs8074995
PRKCA
0.925 0.040 17 66796013 intron variant G/A snv 0.13 5
rs10447760 0.851 0.040 7 114083210 upstream gene variant C/T snv 0.17 4
rs587776703
SCN8A
0.925 0.040 12 51806642 frameshift variant CT/- del 7.0E-06 4
rs11030108
BDNF ; BDNF-AS
1.000 0.040 11 27673917 intron variant A/G snv 0.72 3
rs1187120 0.925 0.040 6 34182850 intergenic variant T/C snv 0.99 3
rs1800557
APP
0.925 0.040 21 25891795 missense variant G/A snv 4.0E-05 4.2E-05 3
rs1938526
ANK3
0.882 0.040 10 60540625 intron variant A/G snv 8.3E-02 3
rs2189814
GRM3
0.925 0.040 7 86702440 intron variant T/A;C snv 3
rs2344484 0.925 0.040 5 135540941 upstream gene variant A/G snv 0.47 3
rs2731880 0.925 0.040 5 36603282 upstream gene variant T/C snv 0.52 3
rs4354668
SLC1A2
0.882 0.040 11 35419429 5 prime UTR variant T/G snv 0.54 3
rs761715536
ADRA2A
1.000 0.040 10 111079092 stop gained G/A;T snv 6.4E-06; 1.3E-05 3
rs781442277
PTRHD1 ; CENPO ; LOC105369164
1.000 0.040 2 24793223 missense variant C/T snv 4.0E-06; 1.2E-05 3
rs1157659 1.000 0.040 11 27736075 intron variant A/G snv 0.37 2
rs115881343
TOMM40
1.000 0.040 19 44899959 intron variant C/G;T snv 2.9E-02 2
rs1245342105
SPTBN1
1.000 0.040 2 54622367 missense variant T/C snv 4.0E-06 2
rs1315695444
SELP
1.000 0.040 1 169611580 missense variant C/G snv 4.0E-06 1.4E-05 2
rs13333659
CBFA2T3
1.000 0.040 16 88972472 intron variant G/T snv 0.13 2
rs1557372 1.000 0.040 21 41460614 downstream gene variant C/T snv 0.40 2
rs17601241
MIR4713HG ; CYP19A1
1.000 0.040 15 51215677 intron variant G/A snv 0.11 8.6E-02 2
rs2162560
DNMT1
1.000 0.040 19 10168778 intron variant G/A snv 0.35 2